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U.S. Department of Health and Human Services

Enforcement Report - Week of October 17, 2012

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Product Detail

Product Description Source Plasma
Recall Number B-1993-12
Classification Class II
Code Info 4140613225; 4140612523; 4140581482; 4140580782; 4140578837; 4140577908; 4140575951; 4140575036; 4140572923; 4140572023; 4140570304; 4140569645; 4140567576; 4140566265; 4140564698; 4140563245; 4140561679; 4140560376; 4140557425; 4140554999; 4140553972; 4140526449; 4140497533; 4140496378; 4140493098; 4140490859; 4140489881; 4140485193; 4140483573; 4140481484; 4140479914; 4140477740; 4140476696; 4140473287; 4140471125; 4140470089; 4140467939; 4140466345; 4140464890; 4140450547; 4140446540; 4140445479; 4140443871; 4140441426; 4140440699; 4140437662; 4140428864; 4140426883; 4140425978; 4140421489; 4140420581; 4140418186; 4140417609; 4140415423; 4140414696; 4140412624; 4140411954; 4140407551; 4140406574; 4140404641; 4140403233; 4140401772; 4140396726; 4140395141; 4140393701; 4140392195; 4140390838; 4140388946; 4140384411; 4140382992; 4140381378; 4140379502; 4140378027; 4140372101; 4140371139; 4140369324; 4140367440; 4140366542; 4140364365; 4140363574; 4140280861; 4140278756; 4140277773; 4140275407; 4140274524; 4140272672; 4140271809; 4140269889; 4140268100; 4140267275; 4140263303; 4140261905; 4140260453; 4140258970; 4140257679; 4140255588; 4140254264; 4140250919; 4140249596; 4140248130; 4140246765; 4140245406; 4140244065; 4140225325; 4140223493; 4140221844; 4140221072; 4140217378; 4140216493; 4140214814; 4140214030; 4140212214; 4140211478; 4140209774; 4140209001; 4140205337; 4140204469; 4140202914; 4140202111; 4140196246; 4140194848; 4140193691; 4140192470; 4140190797; 4140190016; 4140164810; 4140163986; 4140160621; 4140159164; 4140156438; 4140154970; 4140152719; 4140151909; 4140150500; 4140149432; 4140148224; 4140146839; 4140145321; 4140143399; 4140142605; 4140140678; 4140139919; 4140136502; 4140135390; 4140134026; 4140132464; 4140130969; 4140130258; 4140119613; 4140117241; 4140116168; 4140115037; 4140113992; 4140112986; 4140111846; 4140110755; 4140107327; 4140106209; 4140105241; 4140104023; 4140102679; 4140101997; 4140099247; 4140097860; 4140097129; 4140095718; 4140095099; 4140093901; 4140093053; 4140092135; 4140090007; 4140089126; 4140087789; 4140087212; 4140086061; 4140085472; 4140081408; 4140080632; 4140079501; 4140078702; 4140077848; 4140076758; 4140075734; 4140075023; 4140074324; 4140073742; 4140072670; 4140072092; 4140054330; 4140053881; 4140052807; 4140052261; 4140051221; 4140050170; 4140049582; 4140048233; 4140047761; 4140046724; 4140046278; 4140045354; 4140044856; 4140043873; 4140043449; 4140042171; 4140041556; 4140040598; 4140040076; 4140039174; 4140038586; 4140037748; 4140037331; 4140036303; 4140035806; 4140034671; 4140034195; 4140033318; 4140032865; 4140032049; 4140031663; 4140024779; 4140024261; 4140023308; 4140022789; 4140021629; 4140021160; 4140020324; 4140008740;
Product Distributed Qty 227
Reason For Recall Blood products, collected from donors who were previously deferred for high risk behavior, were distributed.

Event Detail

Event Id 54950
Product Type Biologics
Status Terminated
Recalling Firm CSL Plasma, Inc.
City Boca Raton
State FL
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2010-01-29
Initial Firm Notification of Consignee or Public Other
Distribution Pattern IL, Switzerland, Germany
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